Results 1 to 10 of about 21,386 (303)

EBV+ and Kaposi’s Sarcoma Herpesvirus-Associated Multicentric Castleman Disease in a Patient With HIV Infection: A Case Report [PDF]

open access: yesCase Reports in Infectious Diseases
Multicentric Castleman disease is a rare proliferative disease of lymphoid tissue. It has rarely been reported in Asian countries, particularly in HIV-positive patients.
Mai-Yin Huang   +5 more
doaj   +3 more sources

Diagnostic challenges of the idiopathic plasmacytic lymphadenopathy (IPL) subtype of idiopathic multicentric Castleman disease (iMCD): Factors to differentiate from IgG4-related disease. [PDF]

open access: greenJ Clin Pathol
Aims and methods Idiopathic multicentric Castleman disease (iMCD) is currently considered to be classified into three clinical subtypes, including idiopathic plasmacytic lymphadenopathy (IPL), thrombocytopaenia, anasarca, fever, reticulin fibrosis/renal ...
Nishikori A   +15 more
europepmc   +4 more sources

Novel insights and therapeutic approaches in idiopathic multicentric Castleman disease [PDF]

open access: bronzeBlood, 2018
Castleman disease (CD) describes a heterogeneous group of hematologic disorders that share characteristic lymph node histopathology. Patients of all ages present with either a solitary enlarged lymph node (unicentric CD) or multicentric lymphadenopathy ...
David C Fajgenbaum
exaly   +3 more sources

CXCL13 is a predictive biomarker in idiopathic multicentric Castleman disease

open access: yesNature Communications, 2022
Idiopathic multicentric Castleman disease (iMCD) is a life-threatening inflammatory disease requiring immediate intervention, for which the recommended first-line therapy is the Interleukin-6 pathway inhibitor siltuximab.
Sheila K Pierson, Melanie D Mumau
exaly   +3 more sources

Discovery and validation of a novel subgroup and therapeutic target in idiopathic multicentric Castleman disease. [PDF]

open access: goldBlood Advances, 2021
Idiopathic multicentric Castleman disease (iMCD) is a poorly-understood hematologic disorder involving cytokine-induced polyclonal lymphoproliferation, systemic inflammation, and potentially-fatal multi-organ failure.
S. Pierson   +24 more
semanticscholar   +2 more sources

Bone marrow findings of idiopathic Multicentric Castleman disease: A histopathologic analysis and systematic literature review

open access: greenHematological Oncology, 2022
Idiopathic multicentric Castleman disease (iMCD) is a polyclonal lymphoproliferative disorder characterized by constitutional symptoms, generalized lymphadenopathy, cytopenias, and multi‐organ dysfunction due to excessive cytokines, notably Interleukin‐6.
E. Belyaeva   +6 more
semanticscholar   +3 more sources

HHV-8-Associated Multicentric Castleman Disease, a Diagnostic Challenge in a Patient With Acquired Immunodeficiency Syndrome and Fever

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2022
Patients with acquired immunodeficiency syndrome (AIDS) are at an increased susceptibility to pathogens and associated malignancies which can present with a unique constellation of symptoms.
Robert Dunn MS4   +6 more
doaj   +2 more sources

The lymph node transcriptome of unicentric and idiopathic multicentric Castleman disease

open access: yesHaematologica, 2022
Castleman disease is a polyclonal lymphoproliferative disorder characterized by unicentric or multicentric lymphadenopathy with characteristic histomorphological features, in addition to variable inflammatory symptomatology. The molecular mechanisms and
Pedro Horna   +4 more
doaj   +2 more sources

A Review of Genetic Abnormalities in Unicentric and Multicentric Castleman Disease

open access: yesBiology, 2021
Castleman disease (CD) is a rare lymphoproliferative disorder known to represent at least four distinct clinicopathologic subtypes. Large advancements in our clinical and histopathologic description of these diverse diseases have been made, resulting in ...
Alexandra Butzmann   +4 more
doaj   +2 more sources

Idiopathic multicentric Castleman disease developing after a diagnosis of sarcoidosis: A case report and literature review [PDF]

open access: yesRespiratory Medicine Case Reports
A 72-year-old woman presented with an abnormal shadow on chest radiograph. She was histologically diagnosed with sarcoidosis 20 years previously, and prednisolone was initiated 8 years previously.
Takumi Muramatsu   +15 more
doaj   +2 more sources

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